Archive
903 recalls were announced in July 2019.
Of the 903 recalls this month scored against our rubric, 3% are Critical, 17% are Severe.
Which agencies issued them
Dorel Juvenile Group is recalling about 24,000 inclined infant sleepers, including Eddie Bauer and Disney Baby models, due to safety concerns about inclined sleep products.
The Crystal Spoon Corp. is recalling Top Chef Meals Grilled Bison Burgers due to potential E. coli contamination. Consumers should not eat the product.
Topway Enterprises, Inc. is recalling approximately 8,300 pounds of cut salmon due to potential contamination with Listeria monocytogenes. The product was distributed to several southern states.
Brand Castle LLC is recalling Arctic Chill Chocolate Mint Cookie Mix due to potential E. coli contamination in flour.
Topway Enterprises, Inc. is recalling approximately 3,100 pounds of Yellowfin Tuna due to potential contamination with Listeria monocytogenes. The product was distributed across several southern states.
Probar LLC is recalling 14,999 bars of PROBAR MEAL Original Trail Mix because they may contain undeclared milk and soy allergens.
Geritrex, LLC is recalling 6,165 bottles of Gericare Diocto Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.
Brand Castle LLC is recalling Billion Dollar Brownie Mix due to potential E. coli contamination in flour. The product was distributed in ten states.
BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because improperly welded front seatback frames may fold unexpectedly, increasing injury risk in a crash.
Tris Pharma is recalling 2,550 bottles of Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release Suspension due to high out-of-specification results for active ingredients and preservatives.
Geritrex, LLC is recalling Preferred Plus Dioctyl Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.
MORryde is recalling battery trays for Ford F-550 chassis because inadequate welds may allow the tray to detach, creating a road hazard or battery discharge.
Prevost is recalling 2017-2020 H3-45 and X3-45 buses because the engine may overheat and shut down, increasing the risk of a crash or injury.
Probar LLC is recalling 2,908 Superfood Slam meal bars nationwide and in Canada due to undeclared milk and soy allergens.
Pharma-Natural Inc. is recalling Workvie Instant Pain Relieving Roll On due to current good manufacturing practice deviations, including lack of process and cleaning validation.
Zyno Medical LLC is recalling administration sets with inverted pinch clamps that may cause blood to be drawn from patients instead of delivering fluid.
Brand Castle LLC is recalling The Grinch Sugar Cookie Mix with Sprinkles because a supplier reported potential E. coli contamination in the flour used.
Geritrex, LLC is recalling 5,107 bottles of Ritussin DM Children & Adults due to cGMP deviations that may result in microbial contamination.
Frunut Global Commodities LLC is recalling Fruits Du Sud Golden Raisins because the product contains undeclared sulfites.
Geritrex, LLC is recalling Gericare Geri-Tussin DM due to cGMP deviations that may result in microbial contamination.
C & S Wholesale Grocers is recalling Eggland's Best Grade A Large Eggs sold at two Target stores in New York due to a temperature control malfunction during transport.
Xcision Medical Systems is recalling two GammaPod Stereotactic Radiotherapy Systems because a loose bolt caused alignment drift and reduced radiation dose output.
Randox Laboratories is recalling 27 RX Imola instruments after a sensor malfunction caused internal wire melting and scorch damage.
Brand Castle LLC is recalling 46 cases of Million Dollar Cookie Mix due to potential E. coli contamination in flour.
Geritrex, LLC is recalling 8,645 bottles of Diphenhydramine Oral Liquid due to cGMP deviations that may result in microbial contamination.
EL Chilar Huff is recalling Lisy Ground Cinnamon because a sample tested positive for high levels of lead.
Bionpharma Inc. is recalling Clobazam Oral Suspension due to out-of-specification microbial enumeration test results.
Pharma-Natural Inc. is recalling 500 bottles of Double Tussin DM because the product was manufactured with current good manufacturing practice violations.
Gordon Laboratories is recalling 277 boxes of MONSEL'S (Ferric Subsulfate) Solution due to microbial contamination and high iron content.
Geritrex, LLC is recalling Ritussin DM Double Strength cough syrup due to cGMP deviations that may result in microbial contamination.
Geritrex, LLC is recalling Preferred Plus Pharmacy Iron Elixir due to cGMP deviations that may result in microbial contamination.
Philips Medical Systems is recalling 696 BrightView SPECT units because the handcontroller may move spontaneously or continue moving after buttons are released.
Spacelabs Healthcare is recalling the Smart Disclosure System because patient records were printed with waveforms from other patients.
Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Stanley Healthcare is recalling 137 Arial 54315 Network Managers because they caused outages in the Arial nurse call system.
Zevex Incorporated is recalling MOOG Curlin Infusion Administration Sets because they leaked at the filter. The affected sterile sets were distributed to six US states.
Terumo Medical Corporation is recalling 444,000 Sur-vet Needles because a potential loss of package integrity may compromise the sterility of the product.
Laborie Medical Technologies is recalling two U3-3 Solar Blue power supply units due to incorrect labeling and insulation material that does not meet flammability requirements, posing a potential fire hazard.
Baxter Healthcare is recalling 139,680 containers of 0.9% Sodium Chloride Injection due to a lack of assurance of sterility and potential for bags to leak.
Deva Holding AS is recalling Temozolomide Capsules because manufacturing deviations allowed for possible cross-contamination with beta-lactam products.
Philips Medical Systems is recalling 427 BrightView XCT devices because a handcontroller issue may cause uncommanded motions or continued motion after buttons are released.
Siemens is recalling 85 AXIOM Artis dBA units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.
Wegmans is recalling Assorted Whole Wheat Muffins because they may contain pieces of plastic. The recall affects products sold in several northeastern and mid-Atlantic states.
GE Healthcare is recalling 369 MAC VU360 electrocardiographs because they may display incorrect patient IDs or demographics, potentially assigning ECG reports to the wrong patient.
Cardinal Health is recalling specific lots of Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
InfuTronix LLC is recalling Nimbus Administration Sets due to a potential for tube leakage. The recall affects 10,800 units distributed in Massachusetts.
Flowers Foods is recalling 1,467 packages of Flowers Enriched Rolls because they may contain small pieces of hard plastic introduced during production.
Flowers Foods is recalling Krystal 24 Sheet Sandwich Slider Buns because they may contain small pieces of hard plastic introduced during production.
Cardinal Health 200, LLC is recalling Monoject Blunt Cannula 22 G x 1-1/2" (Item code: 8881202389) because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Terumo Medical Corporation is recalling 844,000 Sur-vet Needles because a loss of package integrity may compromise the sterility of the product.
Geritrex, LLC is recalling Gericare Iron Supplement Elixir due to cGMP deviations that may have resulted in microbial contamination.
Flowers Foods is recalling 47,878 packages of hamburger buns sold under multiple brands due to the potential presence of small pieces of hard plastic.
Deva Holding AS is recalling Temozolomide Capsules due to manufacturing deviations that allowed possible cross-contamination with beta-lactam products.
FoodScience Corporation is recalling 256 bottles of DaVinci Laboratories Omega 3-1,000 dietary supplements due to mislabeling and an undeclared allergen.
Terumo Medical Corporation is recalling 563,000 Sur-vet Needles because a potential loss of package integrity may compromise the sterility of the product.
Terumo Medical Corporation is recalling 30,000 units of 23G x 1-inch needles (Lot 180811C) because a potential loss of package integrity may compromise the product's sterility.
London Bridge is recalling infant sock and wrist rattle sets because the sewn-in rattles can detach, posing a choking hazard to young children.
Jelly Belly is recalling Licorice Bridge Mix because the packaging claims 'Gluten Free' but the ingredients list includes wheat flour.
Cardinal Health 200, LLC is recalling Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.
Siemens is recalling 89 Artis zee multi units because a power supply issue may cause the X-ray generator to fail during procedures.
Probar LLC is recalling 61,849 Peanut Butter Chocolate Chip meal bars because they may contain undeclared milk and soy.
CooperSurgical is recalling LEEP Precision Integrated Systems because the foot pedal may fail to operate the cut, coagulate, or blend functions.
Probar LLC is recalling 2,016 Chocolate Coconut bars because they may contain undeclared milk and soy allergens.
Flowers Foods is recalling 4,793 packages of 100% Whole Wheat Hamburger Buns because they may contain small pieces of hard plastic.
Pierce Manufacturing is recalling 174 specific 2019 models because the passenger-side knee air bag may not inflate properly during a crash, increasing injury risk.
Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Cardinal Health is recalling Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.
Brand Castle LLC is recalling Hot Cocoa Cookie Mix because a supplier reported potential E. coli contamination in the flour used.
Mekra Lang is recalling certain Main Mirror Housings for truck cabs because improper adhesive bonding may cause the mirror glass to detach, reducing driver visibility.
Cardinal Health 200, LLC is recalling Monoject Blunt Cannulas because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Wegmans is recalling Large Ultimate Carrot Cakes because they may contain pieces of plastic. The recall affects 20,232 units sold in six states.
Probar LLC is recalling 50,951 Chocolate Coconut meal bars because they may contain undeclared milk and soy allergens.
Cardinal Health is recalling specific lots of Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.
Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Cardinal Health 200, LLC is recalling specific lots of Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Flowers Foods is recalling Laura Lynn and Wonder dinner rolls because they may contain small pieces of hard plastic introduced during production.
Randox Laboratories is recalling RX Daytona instruments due to a sensor malfunction that caused internal wire melting and scorch damage.
Siemens is recalling 19 AXIOM Artis dFC units because a power supply tolerance issue may cause generator failure, preventing X-ray procedures.
Cardinal Health is recalling Monoject Standard Hypodermic Needles due to a manufacturing defect that could compromise the sterility barrier.
Terumo Medical Corporation is recalling 810,000 18G needles due to a potential loss of package integrity that may compromise sterility.
Cardinal Health 200, LLC is recalling Monoject Blunt Cannulas due to a manufacturing defect that could compromise the product's sterility barrier.
Cardinal Health is recalling Monoject 201 Vet Pak Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Brand Castle LLC is recalling Chocolate Mint Chip Cookie Mix due to potential E. coli contamination in flour supplied by a vendor.
Flowers Foods is recalling 46,122 packages of hot dog buns sold under multiple brands because they may contain small pieces of hard plastic.
Vitro is recalling 47,366 aftermarket rear window glass units for various vehicles because improper tempering may result in large fragments that increase injury risk in a crash.
Cardinal Health is recalling specific lots of Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Lupin Pharmaceuticals is recalling 11,832 bottles of Lisinopril and Hydrochlorothiazide tablets because a foreign tablet was found in the product.
Zevex Incorporated is recalling specific lots of MOOG Curlin Infusion Administration Sets because they leaked at the filter.
Flowers Foods is recalling Publix 12 CT Brown & Serve Rolls due to the potential presence of small pieces of hard plastic introduced during production.
Zyno Medical LLC is recalling administration sets where an inverted pinch clamp may cause blood to be drawn from the patient instead of delivering fluid.
Deva Holding AS is recalling Temozolomide Capsules due to manufacturing deviations that allowed possible cross-contamination with beta-lactam products.
Deva Holding AS is recalling Temozolomide Capsules due to manufacturing deviations that allowed possible cross-contamination with beta-lactam products.
Hino is recalling 1,531 model-year 2020 NJ8J, NE8J, and NV8J trucks because exterior mirror glass may detach, reducing driver visibility and increasing crash risk.
National Frozen Foods is recalling Great Value Chopped Spinach due to potential Listeria monocytogenes contamination. The product was distributed in seven states.
Philips Medical Systems is recalling 117 BrightView X devices because a handcontroller issue may cause spontaneous or continued motion.
Cardinal Health 200, LLC is recalling Monoject Blunt Cannula, 20 G x 1-1/2" (Item code: 8881202363), because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Bard Peripheral Vascular is recalling specific Nautilus Delta Port Kits due to a risk of losing the intravascular ECG signal during placement procedures.
The FDA is recalling PROBAR Meal Wholeberry Blast bars because they may contain undeclared milk and soy ingredients. Consumers should discard affected bars and consult their healthcare provider if allergic.
Flowers Foods is recalling Flowers Bratwurst Buns 12 CT because they may contain small pieces of hard plastic introduced during production.
Siemens is recalling one AXIOM Artis TC unit due to a power supply tolerance issue that may cause X-ray generation failure during procedures.
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